HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863830Generated: October 30, 2026
2-Chlorobenzoxazole → 4-(Benzoxazol-2-yl)benzyl alcohol
https://huagongshe.com/reaction/863830
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Benzoxazol-2-yl)benzyl alcohol | HCID 15389017 | — |
Reaction Steps
To 500 ml THF cooled to -78° C. is added butyl lithium (2 eq.) followed by 4-bromobenzyl alcohol (27.2 g; 145 mmol) slowly over 45 minutes in a solution of THF (100 ml) keeping the temperature below -72° C. After 10 minutes following the final addition of the alcohol is added 2-chlorobenzoxazole (23.3 g; 145 mmol) in 25 ml THF slowly over 45 minutes. The temperature is maintained at -78° C. for 1 hour and then warmed to -40° C. for 15 minutes. The reaction is then quenched with 15 ml of acetic acid and allowed to warm to room temperature, diluted with 800 ml ether, washed 3× with H2O and brine, dried (MgSO4) and concentrated in vacuo to obtain a brown oily solid which is washed with 400 ml petroleum ether and filtered to obtain 4-(benzoxazol-2-yl)benzyl alcohol as a tan solid which is used directly in Step B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05561143 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-0faeb24169b14b71b4e23f0df636862f |
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| Source note | uspto-grants-1996_10 |
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